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VIGIMESH Polypropylene Mesh - Indonesia BPOM Medical Device Registration

VIGIMESH Polypropylene Mesh is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21602714030. The device is manufactured by BACTIGUARD (South East Asia) Sdn. Bhd., from Malaysia, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. HOSPI MEDIK INDONESIA.

This page provides comprehensive regulatory information including complete registration details, manufacturer information, authorized representative details, product classification, and related products. Pure Global AI offers free access to 67,600+ Indonesia medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.

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BPOM Registered
Risk Class Kelas Resiko : B
VIGIMESH Polypropylene Mesh
Analysis ID: AKL 21602714030

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Malaysia

Authorized Representative

PT. HOSPI MEDIK INDONESIA

AR Address

Gedung Indra Sentral Blok E-F Lantai 1-2 Jl. Letjen Suprapto No. 60 Kel. Cempaka Putih Barat Kec. Cempaka Putih, Jakarta Pusat 10520

Registration Date

Aug 22, 2024

Expiry Date

Dec 31, 2026

Product Type

Prosthetic Surgical Equipment

Surgical mesh.

Non Electromedic Sterile

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